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Double-sided growth of MoSe2 nanosheets onto hollow zinc stannate (ZnO, ZnSnO3, and SnO2) nanofibers (h-ZTO) for efficient CO2 photoreduction

Authors
Charles, HazinaPawar, Rajendra C.Khan, HarithamChengula, Plassidius J.Lee, Caroline Sunyong
Issue Date
Jun-2023
Publisher
Elsevier Ltd
Keywords
CO2 photoreduction; Hollow zinc stannate nanofiber; Hybrid photocatalyst; MoSe2; Multiple heterojunction
Citation
Journal of Environmental Chemical Engineering, v.11, no.3, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Journal of Environmental Chemical Engineering
Volume
11
Number
3
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/114993
DOI
10.1016/j.jece.2023.109917
ISSN
2213-3437
2213-2929
Abstract
The design of photocatalysts that encourage the conversion of CO2 into useful chemicals has been a recent topic of interest, owing to the consequences of climate change. This study develops h-ZTO/MoSe2 hybrid photocatalysts with multiple heterojunctions using facile electrospinning followed by a solvothermal method. MoSe2 nanosheets are formed inside and outside the h-ZTO hollow nanofibers (NFs), increasing the number of accessible active sites and improving the light-scattering properties, which are fundamental for improved photocatalytic performance. A hybrid photocatalyst was obtained by adjusting the h-ZTO/MoSe2 ratio, which showed significantly higher photocatalytic activity than pure h-ZTO. The morphology, structural, phase composition, and functional characteristics of the synthesized photocatalysts were investigated using FE-SEM, TEM, XRD, XPS, PL, TR-PL, and PEC. The 10 wt% h-ZTO/MoSe2 hybrid photocatalyst demonstrated the effective photocatalytic transformation of CO2 into CO, H2, and CH4 with yielding rates of 140, 64, and 33 µmolg−1h−1, respectively. Furthermore, it exhibited the highest CO2 photoreduction selectivity of 93%. This extraordinary performance can be attributed to the uniform growth of the MoSe2 on the internal and external walls of the hollow nanofibers, which enhanced their light-scattering capabilities and provided abundant active sites for the activation and desorption of CO2 throughout the reaction. © 2023 Elsevier Ltd
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ERICA 첨단융합대학 (ERICA 신소재·반도체공학전공)
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